01 1Alginic Acid Alumina; Hydrated Sodium Bicarbonate
02 2Allopurinol
03 1Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
04 2Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
05 1Apricot
06 1Aprotinin, Bovint
07 1Cetirizine Dihydrochloride
08 2DESMOPRESSIN ACETATE
09 3Desloratadine
10 3Dexibuprofen
11 1Docetaxel (Vattenfri)
12 1Doxycycline Hyclate
13 1Doxycycline Monohydrate
14 2Gimeracil; Oteracil Potassium; Tegafur
15 1Glucosamine Sulfate Potassium Chloride
16 1Loperamide Hydrochloride
17 1Loperamide Hydrochloride; Simethicone
18 8METHOTREXATE
19 5METHOTREXATE (METHOTREXATE SODIUM)
20 25Metadonhydroklorid
21 48Methotrexate
22 8Methotrexate Disodium
23 1Misoprostol
24 2My Firstborn
25 5Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride
26 2Paracetamol
27 2Ranitidine Hydrochloride
28 1Sodium Hyaluronate
29 1Sodium Picosulfate (Monohydrate)
30 4Tegafur; Gimeracil; Oteracyl Potassium
31 1Terbinafinhydrochloride
32 3Xylometazoline Hydrochloride
33 4Ziprasidone Hydrochloride (Anhydrous)
01 3Disphar International Bv
02 5NORDIC GROUP B.V.
03 8NORDIC GRP
04 2NORDIC PHARMA
05 55Nordic Drugs Ab
06 48Nordic Group Bv
07 4Nordic Pharma Bv
08 20Nordic Pharma Gmbh
01 6Capsule
02 1Chewable Tablet
03 2Concentrate For Solution For Infusion
04 2Effervescent Tablet
05 9Film Coated Tablet
06 1Granules
07 4Hard Capsule
08 2INJECTABLE;INJECTION
09 3Inhalation Spray
10 4Injectable Solution
11 8Injectable Solution In Pre-Filled Pen
12 8Injectable Solution In Pre-Filled Syringe
13 1Oral Drops
14 25Oral Solution
15 1Oral Suspension
16 5SOLUTION
17 8SOLUTION;SUBCUTANEOUS
18 37Solution For Injection
19 2Solution For Injection/Infusion
20 16Tablet
01 10.004MG/ML
02 10.015MG/ML
03 10.5mg/ml
04 110.0mg/0.4ml
05 110000KIE/ml
06 3100mg
07 210MG
08 110MG/0.4ML
09 110MG/0.4ML (10MG/0.4ML)
10 510mg
11 110mg/0.4ml
12 110mg/ml
13 110mg;5mg
14 1110mg
15 212.5MG
16 112.5MG/0.5ML (12.5MG/0.5ML)
17 312.5mg
18 212.5mg/0.5ml
19 1120mg
20 1130mg
21 1140mg
22 115.0mg/0.6ml
23 2150mg
24 215MG
25 115MG/0.6ML
26 115MG/0.6ML (15MG/0.6ML)
27 215MG; 4.35MG; 11.8 MG
28 415mg
29 115mg/0.6ml
30 115mg;4.35mg;11.8mg
31 1160mg
32 217.5MG
33 117.5MG/0.7ML (17.5MG/0.7ML)
34 317.5mg
35 217.5mg/0.7ml
36 1170mg
37 1180mg
38 1190mg
39 21mg/ml
40 12.5mg;25mg
41 120.0mg/0.8ml
42 3200mg
43 220MG
44 120MG/0.8ML
45 120MG/0.8ML (20MG/0.8ML)
46 220MG; 5.8MG; 15.8 MG
47 520mg
48 120mg/0.8ml
49 220mg/ml
50 120mg;10mg
51 120mg;5.8mg;15.8mg
52 222.5MG
53 122.5MG/ML (22.5MG/ML)
54 322.5mg
55 222.5mg/0.9ml
56 1250mg
57 225MG
58 125MG/1ML (25MG/1ML)
59 125MG/ML
60 425mg
61 125mg/1.0ml
62 125mg/ml
63 12mg
64 130 mg;15 mg
65 3300mg
66 130mg
67 135mg
68 1400mcg
69 1400mg
70 240mg
71 140mg;20mg
72 145mg
73 2500mg
74 150mg
75 155mg
76 1595mg
77 35mg
78 15mg;2.5mg
79 15mg;50mg
80 1600mg
81 260mg
82 27.5MG
83 17.5MG/0.3ML
84 17.5MG/0.3ML (7.5MG/0.3ML)
85 37.5mg
86 27.5mg/0.3ml
87 17.5mg/ml
88 170mg
89 280mg
90 190mg
91 4Blank
01 5Canada
02 20Spain
03 90Sweden
04 20Switzerland
05 10USA
Regulatory Info : Approved
Registration Country : Sweden
Alginic Acid Alumina; Alginic Acid Alumina; Hydrated Sodium Bicarbonate
Dosage Form : Chewable Tablet
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 30/08/1974
Application Number : 19740830000013
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 100mg
Packaging :
Approval Date : 25/01/1991
Application Number : 19910125000015
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Allopurinol Nordic Drugs
Dosage Strength : 300mg
Packaging :
Approval Date : 25/01/1991
Application Number : 19910125000022
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Alumina, Hydrated; Calcium Carbonate; Sodium Alginate; Sodium Bicarbonate
Dosage Form : Oral Suspension
Brand Name : Gaviscon
Dosage Strength :
Packaging :
Approval Date : 05/02/1982
Application Number : 19820205000135
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm
Dosage Strength : 5mg;50mg
Packaging :
Approval Date : 04/05/1990
Application Number : 19900504000149
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Amiloride Hydrochloride Dihydrate; Hydrochlorothiazide
Dosage Form : Tablet
Brand Name : Amyloferm Mite
Dosage Strength : 2.5mg;25mg
Packaging :
Approval Date : 04/05/1990
Application Number : 19900504000156
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Allowed
Registration Country : Switzerland
Dosage Form : Solution For Injection/I...
Brand Name : Trasylol
Dosage Strength :
Packaging :
Approval Date : 16/03/1977
Application Number : 38837
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection/I...
Brand Name : Trasylol
Dosage Strength : 10000KIE/ml
Packaging :
Approval Date : 13/12/1967
Application Number : 19671213000033
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Acura
Dosage Strength : 10mg
Packaging :
Approval Date : 19/04/2002
Application Number : 20020419000112
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Desloraphar
Dosage Strength : 5mg
Packaging :
Approval Date : 13/09/2012
Application Number : 20110121000033
Regulatory Info : Deregistered
Registration Country : Sweden
